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Job summary
IQVIA is seeking experienced Medical Science Liaisons to support a late-stage AML program. This field-based role engages with investigators, hematologists, oncologists, and other healthcare professionals to exchange scientific data and insights. You will develop relationships with investigators, support investigator-initiated studies, interpret trial data, and communicate evolving standards of care. Travel up to 70% within the assigned territory.
Qualifications
Advanced clinical or scientific degree required; PharmD, MD, DO, PhD, DNP, NP, PA or equivalent strongly preferred.
Minimum of 4 years of MSL experience or relevant clinical experience in hematology/oncology.
Minimum 3 years of experience in hematology/oncology with demonstrated therapeutic expertise.
Proven ability to communicate complex clinical data to diverse audiences.
Proficiency with CRM platforms and MS Office suite.
Responsibilities
Develop and maintain scientific relationships with investigators, KOLs, and hematology/oncology centers across the territory.
Engage in compliant, peer-to-peer scientific discussions regarding AML, MRD, relapse risk, and evolving standards of care.
Support disease-state education, advisory boards, investigator meetings, and compliant medical activities.
Identify medical education needs and facilitate investigator-initiated studies.
Capture stakeholder insights to inform strategic planning and research priorities.
Skills
MSL experience & hematology/oncology
Scientific communication
CRM platforms
MS Office / Teams
Travel readiness
Education
Advanced clinical or scientific degree (PharmD/MD/DO/PhD/DNP/NP/PA)
Tools
CRM platforms
Microsoft Office
Microsoft Teams
Job description
IQVIA is seeking experienced Medical Science Liaisons to support a late-stage AML program. This field-based role engages with investigators, hematologists, oncologists, and other healthcare professionals to exchange scientific data and insights. You will develop relationships with investigators, support investigator-initiated studies, interpret trial data, and communicate evolving standards of care. Travel up to 70% within the assigned territory.